IDS Prolactin
Product Description
The IDS Prolactin assay is an automated in vitro diagnostic device intended for the quantitative, determination of prolactin in human serum and plasma on the IDS system. Results are to be used in conjunction with other clinical and laboratory data as an aid in the diagnosis and monitoring of reproductive and pituitary dysfunction in adult and paediatric populations.
- Standardised to the WHO 4th International Standard (83/573)
- Specific for the 23kDa monomeric form of prolactin
- No sensitivity to high dose hook effect up to 450 000 mIU/L
- No biotin interference by employing direct antibody-solid phase coating principle
- Well-established reference intervals for adult and paediatric populations
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- Saleem M, Martin H, Coates P. Prolactin Biology and Laboratory Measurement: An Update on Physiology and Current Analytical Issues. Clin Biochem Rev. 2018. Feb;39(1):3-16
- Melmed S, et al. Endocrine Society. Diagnosis and treatment of hyperprolactinemia: an Endocrine Society clinical practice guideline. J Clin Endocrinol Metab. 2011 Feb;96(2):273-88.
- Kasum M, et al. Importance of macroprolactinemia in hyperprolactinemia. Eur J Obstet Gynecol Reprod Biol. 2014 Dec;183:28-32. doi: 10.1016/j.ejogrb.2014.10.013. Epub 2014 Oct 20.
- Catli G, et al. Clinical and diagnostic characteristics of hyperprolactinemia in childhood and adolescence. J Pediatr Endocrinol Metab. 2013;26(1-2):1-11. doi: 10.1515/jpem-2012-0327.
- Overgaard M, Pedersen SM. Serum prolactin revisited: parametric reference intervals and cross platform evaluation of polyethylene glycol precipitation-based methods for discrimination between hyperprolactinemia and macroprolactinemia. Clin Chem Lab Med. 2017 Oct 26;55(11):1744-1753.
- Petersenn S. Biochemical diagnosis in prolactinomas: some caveats. Pituitary. 2020 Feb;23(1):9-15.
- Kavanagh L, et al. Specificity and Clinical Utility of Methods for the Detection of Macroprolactin, Clinical Chemistry, Volume 52, Issue 7, 1 July 2006, Pages 1366–1372.
- Product Code: IS-5700
- Number of Tests: 100
- Sample Type: Serum [serum separator tube (SST)] or K2/K3 EDTA plasma
- Sample Volume: 50µL plus dead volume
- Assay Range: 40 to 10,000 mIU/L (Assay Reportable Range: up to 85,000 mIU/L)
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